Kinase Inhibitor Phosphonate Conjugates
a kinase inhibitor and phosphonate technology, applied in the direction of biocide, group 5/15 element organic compounds, drug compositions, etc., can solve the problems of difficult or inefficient intracellular targeting, difficult or inconvenient use of intracellular targets, and reducing the redistribution of drugs to neighboring cells, so as to improve the therapeutic and diagnostic value, the effect of increasing the accumulation and retention of drug compounds
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Synthesis of Representative Compounds of Formulae 1-4
[0618]
[0619] Representative compounds of the invention, e.g., as shown above, can be synthesized according to the following methods. CP-690,550 (3-{4-methyl-3-[methyl-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-amino]-piperidin-1-yl}-3-oxo-propionitrile), can be prepared as described in WO 02 / 096,909 and WO 03 / 048,162. Enolate formation at the α-cyanoamide position using over 2 equivalents of base followed by addition of diethyl phosphonomethyltriflate (prepared according to Tetrahedron Lett., 1986, 27, 1477) yields the desired compound 1.1 shown above. A solvent such as THF, DMF or other anhydrous solvents may be used for this reaction. In case the pyrrole nitrogen interferes with the desired alkylation, a protecting group such as BOC may be introduced before the alkylation reaction. Removal of the BOC group can be accomplished by exposure of the reaction product to TFA as described in Greene, T., Protective Groups In Organic Synthesis, Wi...
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